RenovoRx Enhances Scientific Advisory Board by Adding Esteemed Interventional Oncologist Thierry de Baère, MD, PhD
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Oct 09 2025
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Should l Buy RNXT?
Source: Newsfilter
Appointment of New Advisory Board Member: RenovoRx, Inc. has appointed renowned interventional oncologist Thierry de Baère, MD, PhD, to its Scientific Advisory Board, bringing expertise in targeted oncology therapies and the company's Trans-Arterial Micro-Perfusion (TAMP™) therapy platform.
Innovative Drug-Delivery Technology: RenovoRx is commercializing RenovoCath®, an FDA-cleared drug-delivery device designed to optimize targeted drug delivery for cancer treatment, with ongoing clinical trials for its drug-device combination product candidate, IAG, which has received Orphan Drug Designation for pancreatic and bile duct cancers.
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Analyst Views on RNXT
Wall Street analysts forecast RNXT stock price to rise
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Current: 0.930
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5.63
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12.50
Current: 0.930
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Averages
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About RNXT
RenovoRx, Inc. is a clinical and a commercial biopharmaceutical company. Its lead product RenovoCath a local drug delivery device, targeting high unmet medical needs. RenovoRx’s patented Trans-Arterial Micro-Perfusion (TAMP) therapy platform is designed to ensure targeted therapeutic delivery across the arterial wall near the tumor site to bathe the target tumor. RenovoRx’s novel approach to targeted treatment offers the potential for increased safety, tolerance, and improved efficacy, and to transform the lives of cancer patients by providing innovative solutions to enable targeted delivery of diagnostic and therapeutic agents. In addition to the RenovoCath device, RenovoRx is also evaluating the novel Phase III drug-device combination oncology product candidate (intra-arterial gemcitabine, known as IAG). The combination of intra-arterial infusion of chemotherapy, gemcitabine, and the RenovoCath device is being evaluated for the treatment of locally advanced pancreatic cancer.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- Support for Clinical Trials: The MAB will provide critical insights into RenovoRx's clinical and market strategies, particularly in investigator-initiated trials supported by the company, which are designed to generate meaningful data that may broaden the application of the TAMP platform.
- Market Advancement of Product: With FDA clearance for the RenovoCath device, which enables targeted drug delivery across the arterial wall near tumors, the MAB's feedback will assist the sales and marketing team in bringing RenovoCath to market as a standalone device, enhancing its competitive position.
- Expert Team Composition: Initial members include experienced interventional radiologists such as Dr. Nadine Abi-Jaoudeh from UCI Health and Dr. Mustafa Al-Roubaie from Moffitt Cancer Center, whose expertise will guide RenovoRx's innovative drug delivery approach aimed at improving outcomes for patients with difficult-to-treat cancers.
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- Clinical Data Sharing: Led by Dr. Christopher Laing from Sutter Health, the study is set for presentation on February 6, 2026, emphasizing the significance of real-time intra-arterial pressure monitoring in drug delivery, potentially paving the way for personalized treatment approaches.
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- Formation of Medical Advisory Board: RenovoRx has established a dedicated Medical Advisory Board for RenovoCath, bringing together leading US interventional radiology experts to support clinical and strategic initiatives, thereby advancing the TAMP therapy platform in clinical indications with high unmet medical needs.
- Support for Clinical Trials: The MAB will provide critical insights into RenovoRx's clinical and market strategies, particularly in investigator-initiated trials supported by the company, which are designed to generate meaningful data that may broaden the application of the TAMP platform.
- Market Advancement of Product: With FDA clearance for the RenovoCath device, which enables targeted drug delivery across the arterial wall near tumors, the MAB's feedback will assist the sales and marketing team in bringing RenovoCath to market as a standalone device, enhancing its competitive position.
- Expert Team Composition: Initial members include experienced interventional radiologists such as Dr. Nadine Abi-Jaoudeh from UCI Health and Dr. Mustafa Al-Roubaie from Moffitt Cancer Center, whose expertise will guide RenovoRx's innovative drug delivery approach aimed at improving outcomes for patients with difficult-to-treat cancers.
See More
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- Clinical Data Presentation: RenovoRx will present new clinical data at the Society of Interventional Oncology Annual Meeting on February 6, 2026, focusing on real-time intravascular pressure measurements aimed at optimizing drug delivery in tumors, potentially enhancing treatment outcomes.
- Innovative Research Method: Led by Dr. Christopher Laing from Sutter Health, the study explores real-time intra-arterial pressure measurement methods using the adjustable double-balloon catheter within the TAMP therapy platform, demonstrating potential for optimizing targeted chemotherapy delivery.
- Reliability Validation: Findings indicate that an external pressure transducer provides reliable intra-arterial pressure measurements during TAMP procedures, showing strong correlation with intravascular pressure wire measurements in a porcine model, highlighting opportunities for procedural optimization.
- Clinical Application Prospects: Dr. Ramtin Agah, RenovoRx's Chief Medical Officer, emphasized that routine intra-arterial monitoring could enhance standardization and optimize delivery conditions, potentially improving clinical outcomes and advancing the commercialization of the TAMP therapy platform.
See More
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- Market Potential: The global oncology market is projected to reach $668 billion by 2034, positioning companies like Oncolytics Biotech at the forefront of this rapid growth, particularly in innovative treatments for gastrointestinal cancers, indicating strong market demand and investment appeal.
- Clinical Trial Progress: Oncolytics Biotech's pelareorep achieved a 33% response rate in colorectal cancer patients, significantly surpassing the 6-11% typical response rates of conventional chemotherapy, which not only enhances treatment efficacy but also has the potential to redefine treatment standards in this field, bolstering the company's competitive edge.
- Management Team Upgrade: The recent appointments of John McAdory as Executive Vice President of Strategy and Operations and Yujun Wu as Vice President, Head of Biostatistics, both with extensive clinical trial experience, will provide critical support for Oncolytics' execution of complex multi-country registration trials, ensuring rapid and compliant advancement.
- FDA Trial Design Approval: Oncolytics has secured FDA approval for its Phase 3 trial design for pancreatic cancer, marking the imminent launch of the only immunotherapy registration trial planned for this notoriously difficult-to-treat disease, further solidifying its leadership position in oncology innovation.
See More
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- Market Potential: The global oncology market is projected to reach $668 billion by 2034, positioning Oncolytics Biotech at the forefront of this rapid growth, particularly in the treatment of gastrointestinal cancers through innovative immunotherapy.
- Clinical Trial Progress: Oncolytics Biotech's pelareorep achieved a 33% response rate in colorectal cancer patients, significantly surpassing the 6-11% response rates typical of standard chemotherapy, indicating a potential shift in treatment paradigms.
- Management Team Upgrade: The company appointed two key executives, John McAdory and Yujun Wu, with extensive experience in complex late-stage clinical trials and biostatistics, respectively, which will provide robust support for Oncolytics' clinical trial execution.
- FDA Trial Design Approval: Oncolytics has secured FDA approval for its Phase 3 trial design for pancreatic cancer, making it the only immunotherapy registration trial currently planned for this notoriously difficult-to-treat disease, marking a significant advancement for the company.
See More
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- Research Presentation: RenovoRx's abstract will be showcased at the 2026 SIO Annual Meeting, focusing on optimizing chemotherapy delivery through a double-balloon catheter, highlighting the company's innovative potential in oncology treatment.
- Clinical Data Sharing: Led by Dr. Christopher Laing from Sutter Health, the study is set for presentation on February 6, 2026, emphasizing the significance of real-time intra-arterial pressure monitoring in drug delivery, potentially paving the way for personalized treatment approaches.
- Market Outlook: As an FDA-cleared drug delivery device, RenovoCath is expected to drive the company's commercialization efforts in the oncology market, having generated approximately $900,000 in sales revenue in the first nine months of 2025, indicating growing market demand.
- Strategic Development: RenovoRx is actively exploring further collaborations with medical device commercial partners to meet the increasing demand for RenovoCath, reflecting the company's focus on future market opportunities and strategic positioning.
See More
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- Market Reaction: The significant rise in Bark Inc's stock price reflects investor optimism regarding the company's future, which may also attract more investor attention and enhance market liquidity for the stock.
- Industry Dynamics: In pre-market trading, Signing Day Sports Inc saw a 43.7% increase, while Ping An Biomedical Co Ltd rose 34.3%, highlighting strong market interest in the biotech and sports sectors, which could influence Bark Inc's market positioning.
- Investor Confidence: The rebound in Bark Inc's stock price may bolster investor confidence in the company, especially after recent market volatility, as the acquisition proposal provides new momentum for future growth.
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